US4797342AExpiredUtilityPatentIndex 63
Processes for the preparation of liquid developers with low vapor pressure components
Est. expiryNov 23, 2007(expired)· nominal 20-yr term from priority
G03G 9/12G03G 9/1355
63
PatentIndex Score
4
Cited by
5
References
19
Claims
Abstract
A process for the preparation of liquid developer compositions which comprises mixing a resin with a low vapor pressure oil at elevated temperatures permitting the resin to melt and enabling the formation of a resin oil mixture; thereafter adding to the oil resin mixture at elevated temperatures pigment particles, and stirring until the pigment has become dispersed in the resin; followed by attriting the mixture while cooling, for example, to ambient temperatures; thereafter filtering the aforementioned mixture, and dispersing the product in a low viscosity oil; and subsequently adding to the formed mixture a charge control additive.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A process for the preparation of liquid developer compositions which comprises admixing molten resin components in a vehicle component possessing a vapor pressure of from about 0.01 to about 0.1 millimeter of mercury; thereafter adding thereto pigment particles; subsequently cooling and attriting the aforementioned resulting mixture thereby enabling entrapment of the vehicle in the developer composition; thereafter filtering and dispersing the resulting particles in a low viscosity oil; and adding to the formed composition a charge control director component.
2. A process for the preparation of liquid developer compositions which comprises mixing a resin with a low vapor pressure oil at elevated temperatures permitting the resin to melt and enabling the formation of a resin oil mixture; thereafter adding to the oil resin mixture at elevated temperatures pigment particles, and stirring until the pigment has become dispersed in the resin; cooling the mixture with attrition, thereby enabling entrapment of said oil in the developer composition; thereafter filtering the aforementioned mixture, and dispersing the product in a low viscosity oil; and subsequently adding to the formed mixture a charge control additive.
3. A process in accordance with claim 2 wherein the mixing is accomplished at a temperature of from about 90° to about 110° C.
4. A process in accordance with claim 2 wherein the low vapor pressure oil is present in the mixture in an amount of from about 80 percent by weight to about 90 percent by weight.
5. A process in accordance with claim 2 wherein the vapor pressure of the oil selected is from about 0.01 to about 0.1 millimeter of mercury.
6. A process in accordace with claim 2 wherein the low vapor pressure oil is selected from the group consisting of Isopar V and Magiesol 60.
7. A process in accordance with claim 2 wherein the pigment particles are selected from the group consisting of carbon black, cyan, magenta, yellow, or mixtures thereof.
8. A process in accordance with claim 7 wherein the pigment is present in an amount of from about 3 percent by weight to about 25 percent by weight.
9. A process in accordance with claim 2 wherein subsequent to dispersion of the pigment in the resin particles the mixture is allowed to cool to room temperature over a period of from about 3 to about 5 hours enabling particles with an average diameter of from about 2 to about 3 microns.
10. A process in accordance with claim 2 wherein the charge director is present in an amount of from about 0.01 to about 2 percent by weight.
11. A process in accordance with claim 2 wherein the charge director is selected from the group consisting of polyisobutylene succinimide and lecithin.
12. A process in accordance with claim 2 wherein the developers possess an image transfer efficiency of from about 80 percent to about 99.8 percent.
13. A process in accordance with claim 2 wherein the charge control additive is present in an amount of from about 0.02 percent by weight to about 0.05 percent by weight.
14. A process in accordance with claim 2 wherein the charge director is selected from a group consisting of salts of cadmium, calcium, manganese, magnesium, and zinc salts of heptanoic acid.
15. A process in accordance with claim 2 wherein the charge director is selected from barium, aluminum, cobalt, manganese, zinc, cerium and zirconium salts of 2-ethyl hexanoic acid.
16. A process in accordance with claim 1 wherein the charge director is selected from the group consisting of the barium, aluminum, zinc, copper, lead and iron salts of stearic acid.
17. A process in accordance with claim 1 wherein the charge director is selected from the group consisting of polyisobutylene succinimide and lecithin.
18. A process in accordace with claim 1 wherein the low viscosity oil is Isopar G or Isopar L.
19. A process in accordance with claim 2 wherein the low viscosity oil is Isopar G or Isopar L.Cited by (0)
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